PG-Seq^™ Rapid Kit

The PG-Seq^™ Rapid kit detects whole chromosome aneuploidy along with structural rearrangements such as unbalanced translocations and segmental errors in only 3 hours using an efficient, streamlined workflow. It’s as simple as lyse, whole genome amplify, add indexes and adapters for your choice of sequencing platform with PCR, clean up, quantify, pool, and sequence. Analysis is performed using the 爱游戏平台注册登录 PG-Find^™ software. Test resolution is equivalent to the PG-Seq^™ kit 2.0, with the ability to detect down to 7 Mb deletions and duplications from up to 48 samples. It is available in an Illumina^® or Thermo Fisher^® Ion Torrent^™ sequencer compatible formats. Learn More.